Canonical Allele Identifier: CA349513405

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179417468T>A (hg19) ; chr2:g.178552741T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178552741T>A , CM000664.2:g.178552741T>A	GRCh38
NC_000002.11:g.179417468T>A , CM000664.1:g.179417468T>A	GRCh37
NC_000002.10:g.179125714T>A	NCBI36
NG_011618.3:g.283062A>T , LRG_391:g.283062A>T
NG_051363.1:g.34915T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.82455A>T (TTN)	ENSP00000343764.6:p.Lys27485Asn
ENST00000342175.11:c.63540A>T (TTN)	ENSP00000340554.6:p.Lys21180Asn
ENST00000359218.10:c.63339A>T (TTN)	ENSP00000352154.5:p.Lys21113Asn
ENST00000342175.10:c.63540A>T (TTN)	ENSP00000340554.6:p.Lys21180Asn
ENST00000342992.10:c.82455A>T (TTN)	ENSP00000343764.6:p.Lys27485Asn
ENST00000359218.9:c.63339A>T (TTN)	ENSP00000352154.5:p.Lys21113Asn
ENST00000460472.6:c.62964A>T (TTN)	ENSP00000434586.1:p.Lys20988Asn
ENST00000589042.5:c.90159A>T (TTN) MANE Select	ENSP00000467141.1:p.Lys30053Asn
ENST00000591111.5:c.85236A>T (TTN)	ENSP00000465570.1:p.Lys28412Asn
ENST00000615779.4:c.85236A>T (TTN)	ENSP00000483597.1:p.Lys28412Asn
NM_001256850.1:c.85236A>T (TTN)	NP_001243779.1:p.Lys28412Asn
NM_001267550.2:c.90159A>T (TTN) MANE Select	NP_001254479.2:p.Lys30053Asn
NM_003319.4:c.62964A>T (TTN)	NP_003310.4:p.Lys20988Asn
NM_133378.4:c.82455A>T (TTN)	NP_596869.4:p.Lys27485Asn
NM_133432.3:c.63339A>T (TTN)	NP_597676.3:p.Lys21113Asn
NM_133437.4:c.63540A>T (TTN)	NP_597681.4:p.Lys21180Asn
NR_038271.1:n.447-18559T>A (TTN-AS1)
NR_038272.1:n.2043+10380T>A (TTN-AS1)
XM_011511729.1:c.89256A>T (TTN)	XP_011510031.1:p.Lys29752Asn
XM_011511730.1:c.63150A>T (TTN)	XP_011510032.1:p.Lys21050Asn
XM_011511731.1:c.63009A>T (TTN)	XP_011510033.1:p.Lys21003Asn
XM_017004819.1:c.89052A>T (TTN)	XP_016860308.1:p.Lys29684Asn
XM_017004820.1:c.84450A>T (TTN)	XP_016860309.1:p.Lys28150Asn
XM_017004821.1:c.84447A>T (TTN)	XP_016860310.1:p.Lys28149Asn
XM_017004822.1:c.81489A>T (TTN)	XP_016860311.1:p.Lys27163Asn
XM_017004823.1:c.63105A>T (TTN)	XP_016860312.1:p.Lys21035Asn
XM_024453094.1:c.84600A>T (TTN)	XP_024308862.1:p.Lys28200Asn
XM_024453095.1:c.84597A>T (TTN)	XP_024308863.1:p.Lys28199Asn
XM_024453096.1:c.84030A>T (TTN)	XP_024308864.1:p.Lys28010Asn
XM_024453097.1:c.81372A>T (TTN)	XP_024308865.1:p.Lys27124Asn
XM_024453098.1:c.81291A>T (TTN)	XP_024308866.1:p.Lys27097Asn
XM_024453099.1:c.63054A>T (TTN)	XP_024308867.1:p.Lys21018Asn
XM_024453100.1:c.52908A>T (TTN)	XP_024308868.1:p.Lys17636Asn